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COMPLETED
NCT04718896
PHASE2

A Study to Assess the Pharmacokinetics, Safety, and Efficacy of Two Doses of Bimekizumab in Adolescent Study Participants With Moderate to Severe Plaque Psoriasis

Sponsor: UCB Biopharma SRL

View on ClinicalTrials.gov

Summary

The purpose of the study is to assess th pharmacokinetics (PK) of bimekizumab administered subcutaneously (sc) in adolescents with moderate to severe plaque psoriasis (PSO).

Official title: A Multicenter, Open-Label, Randomized Study to Assess the Pharmacokinetics, Safety, and Efficacy of Two Doses of Bimekizumab in Adolescent Study Participants With Moderate to Severe Plaque Psoriasis

Key Details

Gender

All

Age Range

12 Years - 17 Years

Study Type

INTERVENTIONAL

Enrollment

41

Start Date

2021-04-06

Completion Date

2025-03-12

Last Updated

2026-05-18

Healthy Volunteers

No

Interventions

DRUG

bimekizumab

Study participants will receive subcutaneously administered bimekizumab (BKZ) at pre-specified time points during the study.

Locations (11)

Ps0020 50344

Indianapolis, Indiana, United States

Ps0020 50359

Cypress, Texas, United States

Ps0020 50354

Calgary, Canada

Ps0020 50357

St. John's, Canada

Ps0020 40645

Frankfurt, Germany

Ps0020 40626

Bialystok, Poland

Ps0020 40625

Lodz, Poland

Ps0020 40396

Rzeszów, Poland

Ps0020 40335

Warsaw, Poland

Ps0020 40333

Wroclaw, Poland

Ps0020 40334

Wroclaw, Poland